Joseph A. Sparano
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Articles (17)
Year:
2025
Year:
2025
Year:
2025
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2025
Year:
2024
Year:
2023
Purpose: Endocrine-based therapy is the initial primary treatment option for hormone receptor–positive and human epidermal growth factor receptor 2-negative (HR+/HER2−) metastatic breast cancer (mBC). However, patients eventually experience disease progression due to resistance to endocrine therapy. Molibresib (GSK525762) is a small-molecule inhibitor of bromodomain and extraterminal (BET) family proteins (BRD2, BRD3, BRD4, and BRDT). Preclinical data suggested that the combination of molibresib with endocrine therapy might overcome endocrine resistance. This study aimed to investigate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy [objective response rate (ORR)] of molibresib combined with fulvestrant in women with HR+/HER2− mBC. Patients and Methods: In this phase I/II dose-escalation and dose-expansion study, patients received oral molibresib 60 or 80 mg once daily in combination with intramuscular fulvestrant. Patients enrolled had relapsed/refractory, advanced/metastatic HR+/HER2− breast cancer with disease progression on prior treatment with an aromatase inhibitor, with or without a cyclin-dependent kinase 4/6 inhibitor. Results: The study included 123 patients. The most common treatment-related adverse events (AE) were nausea (52%), dysgeusia (49%), and fatigue (45%). At a 60-mg dosage of molibresib, >90% of patients experienced treatment-related AE. Grade 3 or 4 treatment-related AE were observed in 47% and 48% of patients treated with molibresib 60 mg and molibresib 80 mg, respectively. The ORR was 13% [95% confidence interval (CI), 8–20], not meeting the 25% threshold for proceeding to phase II. Among 82 patients with detected circulating tumor DNA and clinical outcome at study enrollment, a strong association was observed between the detection of copy-number amplification and poor progression-free survival (HR, 2.89; 95% CI, 1.73–4.83; P < 0.0001). Conclusions: Molibresib in combination with fulvestrant did not demonstrate clinically meaningful activity in this study.
Year:
2023
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2023
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2023
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2022
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2022
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2022
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2022
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2021
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2021
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2021
Year:
2021
Collaborators (11)
Elizabeth Chiao
Professor
The University of Texas MD Anderson Cancer Center
Lee Ratner
Professor
Washington University School of Medicine
Jinani Jayasekera
University of Michigan
Ronald Mitsuyasu
Professor
University of California, Los Angeles
Sunil Badve
Vice Chair/ Professor
Emory University
Seema Khan
Professor
Northwestern University Feinberg School of Medicine
Yaguang Wei
Assistant Professor
Icahn School of Medicine at Mount Sinai
Antonio Wolff
Professor of Oncology
Johns Hopkins University
Claudine Isaacs
Professor of Medicine
Georgetown University
Timothy J Whelan
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Missak Haigentz
Professor of Medicine and Chief, Thoracic and Head & Neck Medical Oncology
Rutgers Cancer Institute of New Jersey
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